Carbon dioxide to bio-oil in a bioelectrochemical system-assisted microalgae biorefinery process
Literature Information
Lluís Bañeras, Elisabet Perona-Vico, Andrea G. Capodaglio, Maria Dolors Balaguer, Sebastià Puig
Microbial electrosynthesis (MES) for bioelectro carbon dioxide (CO2) recycling is an interesting and sustainable opportunity to exploit off gases from industrial facilities and convert them into valuable energy sources. In the present study, a two-step process based on coupling a bioelectrochemical system (BES) and heterotrophic microalgae Auxenochlorella protothecoides is proposed to convert carbon dioxide into a biodiesel compatible oil. The MES effluent was further processed in a heterotrophic microalgae batch reactor, where the acetate previously synthesized from CO2 was converted into bio-oil in a subsequent, extraction-free step. Two MES reactors were operated in batch mode at an applied cathodic potential of ā0.8 V vs. SHE (standard hydrogen electrode) for 95 days. The system reached a concentration of up to 13 g Lā1 of acetate (at a maximum production rate of 0.29 g Lā1 dā1). Microbial community analysis revealed the presence of Clostridium spp. in both reactors. In a second stage, the effluent from the biocathode was transferred to microalgae reactors containing A. protothecoides to assess oil production. The bio-oil content was up to 22% w/w (dry weight), sufficient to further explore the feasibility of microalgae-to-oil recovery in the future. According to our estimations, 7.59 kg CO2 can be converted into 1 kg acetate, which can be used to grow heterotrophically 1.11 kg dry algae; an overall balance of 0.03 kg bio-oil produced per kg CO2 captured was assessed. The oil obtained can be further processed to produce a biodiesel compatible with EU requirements for biofuels.
Related Literature
Gold nanoparticle-based competitive colorimetric assay for detection of protein–protein interactions
Charng-Sheng Tsai, Ting-Bin Yu, Chao-Tsen Chen
DOI: 10.1039/B507237A
Thiolate-bridged heterodinuclear platinum–zinc chelates as models for ternary platinum–DNA–protein complexes and zinc ejection from zinc fingers. Evidence from studies using ESI-mass spectrometry
Qin Liu, Melissa Golden, Marcetta Y. Darensbourg, Nicholas Farrell
DOI: 10.1039/B507751F
Water-soluble organic dppz analogues—tuning DNA binding affinities, luminescence, and photo-redox properties
Tim Phillips, Chatna Rajput, Lance Twyman, Ihtshamul Haq, Jim A. Thomas
DOI: 10.1039/B506946G
Enantioselective organocatalytic Michael addition of malonate esters to nitroolefins using bifunctional cinchonine derivatives‡
Jinxing Ye, Darren J. Dixon, Peter S. Hynes
DOI: 10.1039/B508833J
Organogel of an 8-quinolinol platinum(ii) chelate derivative and its efficient phosphorescence emission effected by inhibition of dioxygen quenching
Michihiro Shirakawa, Norifumi Fujita, Takahiro Tani, Kenji Kaneko, Seiji Shinkai
DOI: 10.1039/B506148B
The first ternary tin(ii) nitride: NaSnN
Nicholas S. P. Watney, Zoltán A. Gál, Matthew D. S. Webster, Simon J. Clarke
DOI: 10.1039/B505208D
The elusive phosphorescence of pyrromethene–BF2 dyes revealed in new multicomponent species containing Ru(ii)–terpyridine subunits
Maurilio Galletta, Sebastiano Campagna, Manuel Quesada, Gilles Ulrich, Raymond Ziessel
DOI: 10.1039/B507196H
An organometallic chimie douce approach to new RexW1−xO3 phases
Christian Helbig, Rudolf Herrmann, Franz Mayr, Ernst-Wilhelm Scheidt, Klaus Tröster, Jan Hanss, Hans-Albrecht Krug von Nidda, Gunter Heymann, Hubert Huppertz, Wolfgang Scherer
DOI: 10.1039/B506088E
Polymer vesicles formed by amphiphilic diblock copolymers containing a thermotropic liquid crystalline polymer block
Jing Yang, Daniel Lévy, Wei Deng, Patrick Keller, Min-Hui Li
DOI: 10.1039/B508034G
You might also like
How should waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3) be handled?
Waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3...
How should N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine (CAS: 1318338-47-4) be stored?
N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine should be stored in a tightly sealed c...
What is the market or research trend for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1)?
The market for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1) is...
How should Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) be stored?
Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) ...
What regulatory guidelines apply to 2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3)?
2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3) is regulated under the Glob...
What regulatory guidelines apply to 1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 119462-56-5)?
1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 11946...
Are there alternatives to 5-Fluoro-2-(1-pyrrolidinyl)pyridine (CAS: 1287217-79-1) in synthesis?
Several alternatives can be used in the synthesis of 5-Fluoro-2-(1-pyrrolidinyl)...
What precautions should be taken when handling 1-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione (CAS: 153631-19-7)?
Proper personal protective equipment (PPE) must be worn when handling this compo...
What precautions should be taken when handling 6-Bromoimidazo[1,2-a]pyridin-8-amine (CAS: 676371-00-9)?
When handling 6-Bromoimidazo[1,2-a]pyridin-8-amine, it is important to wear appr...
Are there alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride (CAS: 1049740-22-8) in synthesis?
Alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochlo...











![4-[(2-{2-[2-(2-Aminoethoxy)ethoxy]ethoxy}ethyl)amino]-2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione structure 4-[(2-{2-[2-(2-Aminoethoxy)ethoxy]ethoxy}ethyl)amino]-2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione structure](https://static.chemtradehub.com/structs/209/2093416-31-8-3162.webp)



![2-(7,7-Difluorobicyclo[4.1.0]hept-1-yl)ethanamine structure 2-(7,7-Difluorobicyclo[4.1.0]hept-1-yl)ethanamine structure](https://static.chemtradehub.com/structs/209/2098065-08-6-ff24.webp)